‘They’re not fighting alone’

Standing alongside his parents and his six siblings, Caleb Quick posed for a photo with Brandon Graham and Milton Williams, wearing a gray shirt that stated, “I kicked cancer’s butt.” After the photo, Caleb untangled the yellow wristbands in his right hand and handed them to both players. The bracelets read: For Childhood Cancer Warriors.

“People see football players as heroes,” Caleb said. “So, when the kids look at them they’ll see their heroes wearing the bands to support them.”

When speaking with Caleb, you learn he loves the typical 10-year-old hobbies. He loves to play board games, he loves riding roller coasters, and he loves football. But if you ask him more about himself, you’ll also learn it’s his mission to raise awareness for pediatric cancer after he was diagnosed with leukemia at just 5 years old.

The Quick family isn’t your typical family. In fact, they’re quite hard to miss. Naomi and her husband, John, are raising seven kids all under the age of 17. Their youngest is Hannah, who is 6 years old, then it’s Caleb, 10; Noah, 12; Grace, 13; James, 14; John Daniel, 15; and their oldest daughter, Chara, 16.

The Delaware natives have already combined their mission to raise awareness for pediatric cancer with their love for roller coasters, riding more than 100 of them from Minnesota to Tennessee.

“Our family just kind of draws attention,” Naomi said. “So people kind of look anyway so we use that to our advantage. We would wear foundation T-shirts to the different parks to raise awareness for the different foundations that help childhood cancer. It was raising awareness in this really fun way that didn’t leave people sad. Instead it was more hopeful.”

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Some of these foundations included: B+ Foundation, the Landon Vargas Foundation, Live Like Lucas, Project Outrun, and Kisses for Kyle. Caleb’s Give Kids the World passport, which grants families free access to parks around the country, made this mission possible.

“Childhood cancer is like a roller coaster that no one wants to get on,” Naomi said. “It is full of ups and downs and it makes you feel sick sometimes. And life is a roller coaster in general. But kids should get to ride coasters. Not have to fight cancer.”

Now, the Quicks are ready to raise awareness through the family’s next love: football.

Just months before Caleb was diagnosed with leukemia, his father, John, had just battled ocular melanoma, the most common eye cancer in adults. “Both him and Caleb had genetic testing done and there’s no link between the two,” Naomi said. “So, it’s just like a really bad situation. I don’t know what else to call it, bad luck.”

John was diagnosed in 2019 and was declared cancer free in January 2020 after he was treated by sewing in radiation seeds into his eyeball, the procedure ended up taking the vision from his right eye. Seven months later, Caleb was diagnosed with leukemia.

Naomi remembers bringing Caleb to the emergency room in August 2020, after Caleb was complaining about being tired and having knee pain. She wasn’t expecting her next conversation with the doctor to be something so life changing.

“To have a doctor sit across from you and tell you that you’re really spunky, climbs-all-over-everything, never-settles-down kid has cancer was …” Naomi said before falling silent.

Caleb’s initial hospitalization at the Nemours Children’s Hospital in Wilmington was 22 days. Within the first three days, Naomi said, Caleb couldn’t walk and he was covered from head to toe in bruises.

“It was a really quick progression, and then he developed blood clots unfortunately in his central line, which meant he had to be on blood thinners for a good portion of his treatment as well,” Naomi said. “It was definitely a little bit more complicated than even just the regular treatment.”

By that November, after months of physical therapy and using a walker to move around the house, Caleb rebuilt his muscles and learned to walk again. However, he still has slight residual weakness in one leg from chemotherapy.

Childhood cancer is like a roller coaster that no one wants to get on. It is full of ups and downs and it makes you feel sick sometimes.”

Caleb was in remission within 28 days. But due to a high rate of relapse without the maintenance period of chemotherapy, his treatment lasted another 25 months. His official Ring the Bell date was Oct. 22, 2022. Right after his last dose, he went home to ring the bell in front of his family.

When asked what he wanted to do with his meds and supplies, Caleb responded: “I wanted to burn them.”

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Of course, they didn’t burn the medicine. But they did throw a big party and burned a few papers to signify he was done with his treatment. And throughout the Quick family’s battle with cancer — not once, but twice — they gained an even stronger sense of community.

“Our family has seen those really hard times bring us closer together and make us stronger,” Naomi said. “For all of us, we learned to get through hard times doing it as a family and doing it together. Nobody here had to fight alone, which was good. But that can’t be said for all the other families and so I think it’s really made us more aware and more passionate about fighting on behalf of other families that are going through their own cancer battle.”

On Sept. 19, 2022, Caleb had finished one of the biggest chemo days he had left in his treatment. Later that night, he and his family attended the Eagles’ home opener against the Minnesota Vikings.

The Eagles invited the Quicks to the sideline before the game after learning that they were divided between Vikings and Eagles fans. “It’s split 5-4 in favor of the Eagles, I’m proud to say,” Naomi said. “The Vikings fandom comes from their father’s Minnesota roots.”

Caleb is a fan of both teams. So it was a dream come true for the family to witness both teams in action. Before the game, Graham walked over, welcoming the family with a sweaty hug and words of encouragement.

“He looked at me and he said, ‘My mom had leukemia as a kid and she was told she would never have kids, and look where I am,’” Caleb remembered.

A few weeks earlier, Caleb took part in the Phillies’ Childhood Cancer Awareness Night, and got to meet then-first lady Jill Biden.

Two weeks later, toward the end of his treatment, Caleb took a dive in health. The cumulative effect of over two years of chemo had taken its toll on his body. He developed three different viral infections and four different bacterial infections.

“It was a little scary, and I just remember thinking to myself, replaying those words that Brandon had spoken. He did say that, ‘With God, all things are possible. He’s a fighter, he’s going to make it,’” Naomi recalled. “And I just held onto that because I needed that encouragement. And to have it come from somebody who is a hero to the community, it was a really special interaction.”

Football has always played a special role for the Quick family, through both Caleb’s and John’s cancer battles. For John, it was an escape. For Caleb, it was an inspiration.

“John was diagnosed right in the middle of the football season,” Naomi said. “So, football games were this way that we could have normal family time. It was just kind of an escape from reality during both of their cancer fights. Meanwhile, football was an inspiration for Caleb to walk again.

“Football was the saving grace, and like I said, when he lost his ability to walk, he would say, ‘Mom, I can’t play in the NFL anymore.’ He wants to play in the NFL and he can’t do that if he can’t walk.”

During the 2022 season, Eagles wide receiver DeVonta Smith wore a yellow wristband given to him by 10-year-old Nicholas Purificato, who was battling Ewing’s sarcoma, a rare bone cancer. Starting that October, Smith wore the bracelet every day at practice and during games to support his fight.

One day, Caleb spotted the yellow bracelet and looked up at his mom and said, “Mom, No. 6, Smith, he cares about kids like me. Look at those bands,” Naomi recalled.

At that moment, she ordered similar yellow bands for her son, with the words “For childhood cancer warriors” and a gold ribbon engraved on them.

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At last year’s Big Climb, a fundraiser for the Leukemia Lymphoma Society, Caleb met Milton Williams and Tarron Jackson, a pair of former Eagles defensive ends. Williams, who signed with the New England Patriots this offseason, shared his story about his mother’s battle with breast cancer and proudly accepted Caleb’s bracelet. A few months later, Williams was still wearing the bracelet.

“We offered him one and then he took a whole bag to the locker room and passed them out,” Naomi said. “We ended up seeing the team pictures later in August and he was wearing them in his team pictures. Caleb was showing it to all of his friends and family. It was a cool moment.”

But it’s not just Caleb and Naomi’s mission to raise awareness for pediatric cancer. After watching Caleb battle leukemia at such a young age, his siblings have made it their mission as well.

People see football players as heroes. So, when the kids look at them they’ll see their heroes wearing the bands to support them.”

“Since we know how hard it is for kids to go through cancer, we know that other families who have to go through the same thing, it’s hard for them too,” said Caleb’s sister Grace. “So, when you raise awareness, those families know that you care.”

Caleb’s older brother J.D. added: “If they’re wearing bands and they’re asked by a reporter why they’re wearing them, then people start to wonder more about cancer because a lot of people don’t know a whole lot about cancer until somebody they know has had it.”

The Quick family’s ultimate goal is to get bracelets to all 32 teams in the NFL.

“September is childhood cancer awareness month and it really doesn’t get as much publicity as some other awareness months do, which is odd,” Naomi said. “It seems to be that you have to be in this world to know a lot about it. So, our hope was that if we could get to all 32 teams, then kids across the country, no matter who they’re rooting for, will know that there are people rooting for them. Every child deserves that. Every kid deserves to know that they’re not fighting alone.”

As of October, Caleb was moved to annual visits after his three-year off treatment lab results came back perfect.